Intramolecular Cycloaddition of Imines of Cysteine Derivatives

Detalhes bibliográficos
Autor(a) principal: Cabral, Ana M. T. D. P. V.
Data de Publicação: 1998
Outros Autores: Gonsalves, António M. d'A. Rocha, Melo, Teresa M. Pinho e
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10316/13018
https://doi.org/10.3390/30300060
Resumo: Azomethine ylides were generated from Schiffs bases of S-allylcysteine methyl ester and their intramolecular 1,3-dipolar cycloadditions were studied. These reactions led to the synthesis of thieno[3,4-b]pyrrole derivatives in good yield
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spelling Intramolecular Cycloaddition of Imines of Cysteine DerivativesThieno[3; 4-b]pyrrole derivativesSynthesisAzomethine ylides were generated from Schiffs bases of S-allylcysteine methyl ester and their intramolecular 1,3-dipolar cycloadditions were studied. These reactions led to the synthesis of thieno[3,4-b]pyrrole derivatives in good yieldMolecular Diversity Preservation International1998-02-18info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://hdl.handle.net/10316/13018http://hdl.handle.net/10316/13018https://doi.org/10.3390/30300060engMolecules. 3:3 (1998) ) 60-631420-3049Cabral, Ana M. T. D. P. V.Gonsalves, António M. d'A. RochaMelo, Teresa M. Pinho einfo:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2020-11-06T17:00:28Zoai:estudogeral.uc.pt:10316/13018Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T21:01:42.105447Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv Intramolecular Cycloaddition of Imines of Cysteine Derivatives
title Intramolecular Cycloaddition of Imines of Cysteine Derivatives
spellingShingle Intramolecular Cycloaddition of Imines of Cysteine Derivatives
Cabral, Ana M. T. D. P. V.
Thieno[3; 4-b]pyrrole derivatives
Synthesis
title_short Intramolecular Cycloaddition of Imines of Cysteine Derivatives
title_full Intramolecular Cycloaddition of Imines of Cysteine Derivatives
title_fullStr Intramolecular Cycloaddition of Imines of Cysteine Derivatives
title_full_unstemmed Intramolecular Cycloaddition of Imines of Cysteine Derivatives
title_sort Intramolecular Cycloaddition of Imines of Cysteine Derivatives
author Cabral, Ana M. T. D. P. V.
author_facet Cabral, Ana M. T. D. P. V.
Gonsalves, António M. d'A. Rocha
Melo, Teresa M. Pinho e
author_role author
author2 Gonsalves, António M. d'A. Rocha
Melo, Teresa M. Pinho e
author2_role author
author
dc.contributor.author.fl_str_mv Cabral, Ana M. T. D. P. V.
Gonsalves, António M. d'A. Rocha
Melo, Teresa M. Pinho e
dc.subject.por.fl_str_mv Thieno[3; 4-b]pyrrole derivatives
Synthesis
topic Thieno[3; 4-b]pyrrole derivatives
Synthesis
description Azomethine ylides were generated from Schiffs bases of S-allylcysteine methyl ester and their intramolecular 1,3-dipolar cycloadditions were studied. These reactions led to the synthesis of thieno[3,4-b]pyrrole derivatives in good yield
publishDate 1998
dc.date.none.fl_str_mv 1998-02-18
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://hdl.handle.net/10316/13018
http://hdl.handle.net/10316/13018
https://doi.org/10.3390/30300060
url http://hdl.handle.net/10316/13018
https://doi.org/10.3390/30300060
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Molecules. 3:3 (1998) ) 60-63
1420-3049
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.publisher.none.fl_str_mv Molecular Diversity Preservation International
publisher.none.fl_str_mv Molecular Diversity Preservation International
dc.source.none.fl_str_mv reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
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